Reaction Details |
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Target | Methionine aminopeptidase 2 |
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Ligand | BDBM50141730 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_105142 |
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IC50 | 20±n/a nM |
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Citation | Sheppard, GS; Wang, J; Kawai, M; BaMaung, NY; Craig, RA; Erickson, SA; Lynch, L; Patel, J; Yang, F; Searle, XB; Lou, P; Park, C; Kim, KH; Henkin, J; Lesniewski, R 3-Amino-2-hydroxyamides and related compounds as inhibitors of methionine aminopeptidase-2. Bioorg Med Chem Lett14:865-8 (2004) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Methionine aminopeptidase 2 |
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Name: | Methionine aminopeptidase 2 |
Synonyms: | Initiation factor 2-associated 67 kDa glycoprotein | MAP 2 | MAP2_HUMAN | METAP2 | MNPEP | MetAP 2 | Methionine aminopeptidase 2 (MetAP2) | Methionine aminopeptidases (HsMetAP2) | P67EIF2 | Peptidase M 2 | p67 |
Type: | Enzyme |
Mol. Mass.: | 52884.45 |
Organism: | Homo sapiens (Human) |
Description: | P50579 |
Residue: | 478 |
Sequence: | MAGVEEVAASGSHLNGDLDPDDREEGAASTAEEAAKKKRRKKKKSKGPSAAGEQEPDKES
GASVDEVARQLERSALEDKERDEDDEDGDGDGDGATGKKKKKKKKKRGPKVQTDPPSVPI
CDLYPNGVFPKGQECEYPPTQDGRTAAWRTTSEEKKALDQASEEIWNDFREAAEAHRQVR
KYVMSWIKPGMTMIEICEKLEDCSRKLIKENGLNAGLAFPTGCSLNNCAAHYTPNAGDTT
VLQYDDICKIDFGTHISGRIIDCAFTVTFNPKYDTLLKAVKDATNTGIKCAGIDVRLCDV
GEAIQEVMESYEVEIDGKTYQVKPIRNLNGHSIGQYRIHAGKTVPIVKGGEATRMEEGEV
YAIETFGSTGKGVVHDDMECSHYMKNFDVGHVPIRLPRTKHLLNVINENFGTLAFCRRWL
DRLGESKYLMALKNLCDLGIVDPYPPLCDIKGSYTAQFEHTILLRPTCKEVVSRGDDY
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BDBM50141730 |
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n/a |
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Name | BDBM50141730 |
Synonyms: | (2S,3R)-3-Amino-5-ethylsulfanyl-2-hydroxy-pentanoic acid methyl-naphthalen-1-ylmethyl-amide | CHEMBL168717 |
Type | Small organic molecule |
Emp. Form. | C19H26N2O2S |
Mol. Mass. | 346.487 |
SMILES | CCSCC[C@@H](N)[C@H](O)C(=O)N(C)Cc1cccc2ccccc12 |
Structure |
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